A WrapAround Case Management Program for Youth Injured by Violence

July 4, 2013 updated by: Dr. Carolyn Snider, University of Manitoba

A WrapAround Case Management Program for Youth Injured by Violence: A Feasibility Study

This is a feasibility study of a WrapAround Case Management Program for Youth Injured by Violence. Youth (aged 10-24) who have been injured by violence and visit the emergency department will be offered a support worker who will provide WrapAround Case Management. This study is designed to assess the feasibility of recruitment, enrollment and follow-up.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

8

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Manitoba
      • Winnipeg, Manitoba, Canada, R3P 3E4
        • Winnipeg Health Sciences Centre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years to 24 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Age 10 - 24 and
  2. Presentation to an ED or trauma floor with an injury caused by violence (defined as an injury inflicted by someone else and one of a gunshot wound, stab wound, injury due to blunt object, or injury due to bodily force).

Exclusion Criteria:

  1. Unable to consent due to language or brain injury,
  2. Sexual assault,
  3. Child Abuse
  4. Self-Inflicted Injury,
  5. Subject is under arrest or
  6. Non-resident of Winnipeg.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: WrapAround Care
Youth Injured by Violence will be paired with a support worker who has extensive experience working with youth affected by violence.It is important to note that the wraparound concept involves individualized care planning and management. As such, the specific care plan will be different for each participant. Through early intensive meetings, they will develop a mentoring relationship. They will work with the youth to develop a support team, which may include family, teachers, child welfare workers and truly anyone the youth has decided can help them in their path to making positive choices.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To estimate the recruitment rate of an ED referral program for injured youth
Time Frame: 6 months
We will evaluate the proportion of eligible patients who are identified for enrolment and any biases in subject identification
6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
To identify barriers to participation in a hospital-based case management program
Time Frame: 6 months
6 months
To determine the average number of contacts and amount of time required per participant
Time Frame: 6 months
6 months
To estimate the rates of follow-up among those successfully recruited
Time Frame: 6 months
6 months
To determine the most appropriate way to notify the case manager of an eligible participant
Time Frame: 6 months
6 months
To determine the most successful enrollment strategy for retention of participants
Time Frame: 6 months
6 months
To determine level of engagement between the case manager and youth
Time Frame: 6 months
6 months
To determine the most appropriate method of follow-up
Time Frame: 6 months
6 months
To determine the impact in violence-related attitudes and behaviours among participants
Time Frame: 6 months
6 months
To determine the impact on recurrent intentional injury amongst participants
Time Frame: 6 months
6 months
To determine the impact on modifiable risk factors
Time Frame: 6 months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carolyn E Snider, MD MPH, University of Manitoba

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2012

Primary Completion (Actual)

June 1, 2013

Study Completion (Actual)

June 1, 2013

Study Registration Dates

First Submitted

December 13, 2012

First Submitted That Met QC Criteria

December 13, 2012

First Posted (Estimate)

December 18, 2012

Study Record Updates

Last Update Posted (Estimate)

July 8, 2013

Last Update Submitted That Met QC Criteria

July 4, 2013

Last Verified

July 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • H2012:133

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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